Juvenile myoclonic epilepsy (JME) is an epileptic condition that develops in children and adolescents, invariably between the ages of 8 and 26 with most of the seizures occurring between the ages ...

After a few weeks, I was diagnosed with Juvenile Myoclonic Epilepsy. People tend to assume that epileptic seizures are triggered by flashing lights, but that’s not the case for me. Mine are ...

Juvenile myoclonic epilepsy was diagnosed and treatment with valproic acid initiated, which alleviated the myoclonus and decreased the frequency of the seizures. Several months later, the patient ...

A recent report has described the use of video-electroencephalography (video-EEG) in the management of patients with atypical juvenile myoclonic epilepsy (JME). The work highlights the importance ...

Cedars Sinai explains that this includes, but is not limited to, frontal lobe epilepsy, juvenile myoclonic epilepsy, or ...

These children show myoclonic jerks and/or epilepsy with generalized tonic-clonic seizures only in response to a visual stimulus. Visually induced and spontaneous seizures, with or without a ...

LOOKING AT THAT WEEKEND FORECAST BECAUSE HAPPENING THIS WEEKEND, IT’S THE 2025 WALK FOR EPILEPSY. THIS IS THE TIME TO RAISE AWARENESS AND MONEY TO SUPPORT THE EPILEPSY COMMUNITY. JOINING US NOW WITH ...

especially juvenile myoclonic; Lennox-Gastaut syndrome; and refractory epilepsy in children and adults. Data are emerging on possible uses of levetiracetam outside the realm of epilepsy because of ...